# ICOSAPENT ETHYL

NDC: 16714-636
Generic name: Icosapent ethyl
Labeler / Manufacturer: Northstar Rx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20250701

FDA application: ANDA216811

## Active ingredients

- ICOSAPENT ETHYL: 1 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16714-636"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16714-636
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b5b0b1ae-29ab-43a5-9e6d-24374d961399